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May 30, 2017; 88 (22) Article

White matter microstructure, cognition, and molecular markers in fragile X premutation females

Annie L. Shelton, Kim M. Cornish, David Godler, Quang Minh Bui, Scott Kolbe, Joanne Fielding
First published May 5, 2017, DOI: https://doi.org/10.1212/WNL.0000000000003979
Annie L. Shelton
From the School of Psychological Sciences and Monash Institute of Cognitive and Clinical Neurosciences (A.L.S., K.M.C., J.F.), Monash University; Cyto-molecular Diagnostic Research Laboratory (D.G.), Murdoch Childrens Research Institute; and Centre for Epidemiology and Biostatistics (Q.M.B.), Melbourne School of Population and Global Health, Department of Anatomy and Neuroscience (S.K.), and Department of Medicine (J.F.), University of Melbourne, VIC, Australia.
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Kim M. Cornish
From the School of Psychological Sciences and Monash Institute of Cognitive and Clinical Neurosciences (A.L.S., K.M.C., J.F.), Monash University; Cyto-molecular Diagnostic Research Laboratory (D.G.), Murdoch Childrens Research Institute; and Centre for Epidemiology and Biostatistics (Q.M.B.), Melbourne School of Population and Global Health, Department of Anatomy and Neuroscience (S.K.), and Department of Medicine (J.F.), University of Melbourne, VIC, Australia.
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David Godler
From the School of Psychological Sciences and Monash Institute of Cognitive and Clinical Neurosciences (A.L.S., K.M.C., J.F.), Monash University; Cyto-molecular Diagnostic Research Laboratory (D.G.), Murdoch Childrens Research Institute; and Centre for Epidemiology and Biostatistics (Q.M.B.), Melbourne School of Population and Global Health, Department of Anatomy and Neuroscience (S.K.), and Department of Medicine (J.F.), University of Melbourne, VIC, Australia.
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Quang Minh Bui
From the School of Psychological Sciences and Monash Institute of Cognitive and Clinical Neurosciences (A.L.S., K.M.C., J.F.), Monash University; Cyto-molecular Diagnostic Research Laboratory (D.G.), Murdoch Childrens Research Institute; and Centre for Epidemiology and Biostatistics (Q.M.B.), Melbourne School of Population and Global Health, Department of Anatomy and Neuroscience (S.K.), and Department of Medicine (J.F.), University of Melbourne, VIC, Australia.
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Scott Kolbe
From the School of Psychological Sciences and Monash Institute of Cognitive and Clinical Neurosciences (A.L.S., K.M.C., J.F.), Monash University; Cyto-molecular Diagnostic Research Laboratory (D.G.), Murdoch Childrens Research Institute; and Centre for Epidemiology and Biostatistics (Q.M.B.), Melbourne School of Population and Global Health, Department of Anatomy and Neuroscience (S.K.), and Department of Medicine (J.F.), University of Melbourne, VIC, Australia.
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Joanne Fielding
From the School of Psychological Sciences and Monash Institute of Cognitive and Clinical Neurosciences (A.L.S., K.M.C., J.F.), Monash University; Cyto-molecular Diagnostic Research Laboratory (D.G.), Murdoch Childrens Research Institute; and Centre for Epidemiology and Biostatistics (Q.M.B.), Melbourne School of Population and Global Health, Department of Anatomy and Neuroscience (S.K.), and Department of Medicine (J.F.), University of Melbourne, VIC, Australia.
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Citation
White matter microstructure, cognition, and molecular markers in fragile X premutation females
Annie L. Shelton, Kim M. Cornish, David Godler, Quang Minh Bui, Scott Kolbe, Joanne Fielding
Neurology May 2017, 88 (22) 2080-2088; DOI: 10.1212/WNL.0000000000003979

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This article has a correction. Please see:

  • White matter microstructure, cognition, and molecular markers in fragile X premutation females - September 26, 2017
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Abstract

Objective: To examine the interrelationships between fragile X mental retardation 1 (FMR1) mRNA and the FMR1 exon 1/intron 1 boundary methylation, white matter microstructure, and executive function, in women with a FMR1 premutation expansion (PM; 55–199 CGG repeats) and controls (CGG < 44).

Methods: Twenty women with PM without fragile X-associated tremor/ataxia syndrome (FXTAS) and 20 control women between 22 and 54 years of age completed this study. FMR1 mRNA and methylation levels for 9 CpG sites within the FMR1 exon 1/intron 1 boundary from peripheral blood samples were analyzed. To measure white matter microstructure, diffusion-weighted imaging was used, from which fractional anisotropy (FA) and mean diffusivity (MD) values from anatomic regions within the corpus callosum and cerebellar peduncles were extracted. Executive function was assessed across a range of tasks.

Results: No differences were revealed in white matter microstructure between women with PM and controls. However, we reveal that for women with PM (but not controls), higher FMR1 mRNA correlated with lower MD values within the middle cerebellar peduncle and Paced Auditory Serial Addition Test scores, higher methylation of the FMR1 exon 1/intron 1 boundary correlated with lower MD within the inferior and middle cerebellar peduncles and longer prosaccade latencies, and higher FA values within the corpus callosum and cerebellar peduncle regions corresponded to superior executive function.

Conclusions: We provide evidence linking white matter microstructure to executive dysfunction and elevated FMR1 mRNA and FMR1 exon 1/intron 1 boundary methylation in women with PM without FXTAS. This suggests that the FXTAS phenotype may not be distinct but may form part of a spectrum of PM involvement.

GLOSSARY

AR=
activation ratio;
BDS=
Behavioural Dyscontrol Scale;
CC=
corpus callosum;
COWAT=
Controlled Oral Word Association Test;
FA=
fractional anisotropy;
FDR=
false discovery rate;
FMR1=
fragile X mental retardation 1;
FXTAS=
fragile X-associated tremor/ataxia syndrome;
ICP=
inferior cerebellar peduncle;
MCP=
middle cerebellar peduncles;
MD=
mean diffusivity;
PASAT=
Paced Auditory Serial Addition Test;
PM=
premutation;
ROI=
region of interest;
SCP=
superior cerebellar peduncle;
SDMT=
Symbol Digit Modality Test

Footnotes

  • Go to Neurology.org for full disclosures. Funding information and disclosures deemed relevant by the authors, if any, are provided at the end of the article.

  • Editorial, page 2070

  • Supplemental data at Neurology.org

  • Received July 27, 2016.
  • Accepted in final form February 14, 2017.
  • © 2017 American Academy of Neurology
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